Classifications

• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
  • D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D01F6/18—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide

Definitions

• This invention relates to a wet-spinning process for making acrylonitrile polymer filaments.
• the tenacity of the filaments is greatly improved by stretching to molecularly orient the polymer molecules and at least partially collapse these voids. To more fully collapse these voids the filaments may be dried at rather high temperatures under tension, thereby forming a more dense filamentary structure.
• the tenacity of the filaments is generally satisfactory with such after treatment. However, tenacity is primarily a longitudinal property of the filaments; and satisfactory tenacity, alone, is not the full answer to the attainment of filaments having an optimum balance of properties. In many end uses, the abrasion resistance and the resistance to break upon being flexed (flex life) are highly important.
• Such properties may be regarded as lateral properties as distinguished from longitudinal properties. While drying under tension gives the illusion of forming filaments without voids, the voids are merely collapsed. Although the collapsed voids do not detract from the longitudinal properties of the filaments to any significant extent, it has been found that lateral stresses cause filaments to splinter or break. In other words, filaments having voids which are merely collapsed are laterally weak.
• micropores present in filaments produced by ordinary wet-spinning techniques as they leave the coagulating bath are more or less spherical.
• the distances across these spaces are ordinarily about 250 A. to 3000 A. or greater.
• the frequency of occurrence of the micropores in the filaments produced by ordinary wet-spinning techniques employing aqueous coagulating baths can be estimated under an electron microscope and is usually 35-90 ⁇ 10 14 per gram of polymer.
• the properties of the filaments can be improved substantially by subjecting the filaments to an annealing operation.
• Annealing can be accomplished by placing the acrylonitrile polymer filaments in a closed chamber, subjecting them to a high temperature and pressure in the presence of wet steam and then evacuating the chamber. This treating cycle is repeated as many times as needed. It will be appreciated that this annealing operation is expensive and time consuming. However, omitting the annealing step in the after treatment of conventionally wet spun acrylic filaments results in filaments having a tendency to splinter or fibrillate; and hence, the filaments have a low abrasion resistance.
• This invention provides a process for wet-spinning acrylonitrile polymer filaments. More specifically, a solution of acrylonitrile polymer containing at least 30 microequivalents per gram strong acid groups in N,N-dimethylacetamide (DMAc) or dimethylformamide (DMF), preferably DMAc, is extruded into a water/N,N-dimethylacetamide or water/dimethylformamide coagulation bath. Polymer composition and coagulation bath composition are correlated to result in a calculated Rho value (as hereinafter defined) of at least 0.60. This results in filaments which can be rendered commercially useful without batch annealing or which, if desired, can be conventionally annealed to provide superior properties.
• Rho value as hereinafter defined
• the polymer spun in accordance with the present invention will be a polymer of acrylonitrile which may be copolymerized with 0% to 15% by weight of a neutral comonomer--i.e., a comonomer such as vinyl acetate or methyl methacrylate which contains no strong acid groups.
• a neutral comonomer--i.e., a comonomer such as vinyl acetate or methyl methacrylate which contains no strong acid groups.
• the polymer will contain 30 to 250 microequivalents/gm strong acid groups (sulfate or sulfonate groups) which may be provided by the redox couple polymerization process or by copolymerization with acidic comonomers (such as sodium para-sulfophenyl methallylether (SPME), sodium methyl sulfonate, or sodium styrene sulfonate) or both.
• acidic comonomers such as sodium para-sulfophenyl methallylether (SPME), sodium methyl sulfonate, or sodium styrene sulfonate
• SPME sodium para-sulfophenyl methallylether
• Rho values as sodium styrene sulfonate
• the polymer is dissolved in N,N-dimethylacetamide (DMAc) or dimethylformamide (DMF) or mixtures thereof which may contain 0% to 3% by weight water.
• the solution is extruded through a spinnerette (which may be of conventional design) into a coagulating bath.
• the coagulating bath is maintained at a temperature of from 10° C. to 32° C. and consists essentially of DMAc or DMF (preferably DMAc) or mixtures thereof and water.
• the molar ratios of solvent to water which will result in the required Rho values are believed related to the rate of water diffusion from the coagulating bath into the polymer solution and the rate of polymer phrase separation. It is believed that the water to solvent mole ratio controls the rate of diffusion and that the level of polymer strong acid groups controls the rate of polymer phase separation.
• a water/solvent mole ratio of about ( ⁇ 0.2) 2/1 appears optimum. At this ratio all the water is associated with the solvent and the system behaves as a single phase coagulant which should provide the slowest rate of diffusion into the coagulating fiber.
• Rho values are calculated by the formula:
• R r 1 +r 2 -(r 1 ⁇ r 2 ); r 1 being the rate of water diffusion and being equal to e.sup.[(2-W/S)2] where W/S is the water to solvent mole ratio in the coagulating bath; and r 2 is the rate of polymer phase separation which is equal to e.sup.[(microequivalents per gram of sulfate and sulfonate groups-95)/95].
• the polymer composition and water to solvent ratio in the coagulation bath are correlated such that fiber density is at least 0.60, preferably at least 0.8 and most preferably 1.0 or higher.
• Higher Rho values may be less practical because of the expense of copolymer containing very high levels of strong acid groups and/or the tendency of filaments to stick together (marry) in coagulation baths having low W/S ratios.
• Rho values are significantly higher than values calculated for conventional wet spinning processes using DMAc or DMF dope and coagulation bath solvent systems.
• Those skilled in the wet-spinning art will recognize that the present process is primarily characterized by use of copolymers with higher strong acid group levels and/or lower water to solvent ratios in the coagulation bath which combination translates to higher calculated Rho values.
• Those higher Rho values are believed to correlate with higher as-spun fiber densities (a reduced volume of voids in the fiber matrix) but applicants do not intend to be bound by this theory because fiber density measurement techniques to confirm the theory are not conveniently available.
• the polymer will be an acrylonitrile polymer containing from 0% to 15% by weight vinyl acetate and having a total of 30 to 250 microequivalents per gram sulfate and/or sulfonate groups.
• These strong acid groups can conveniently be provided by the acrylonitrile redox couple polymerization or by copolymerization of an acidic comonomer.
• the polymer will be extruded as a 20% to 26% by weight solution in which the solvent is DMAc or DMF containing 0% to 3% water by weight.
• the coagulation bath will consist essentially of DMAc or DMF and water in a ratio correlated with copolymer strong acid group content to provide the required Rho value.
• the bath will be maintained at a temperature of from 10° C.-32° C.
• Jet stretch which is the speed of the first stretching roll set contacted by the filaments on exiting the spinnerette divided by the velocity of the polymer solution through the spinnerette, is controlled between 0.2 and 1.0, preferably 0.4 to 0.6. At lower jet stretch, processing difficulties are encountered and at higher jet stretch, void sizes tend to increase.
• Wet stretch between 2 ⁇ and 8 ⁇ is provided by feeding the filaments into a second higher speed roll set and stretching the wet filaments. At lower wet stretch, low fiber strength results and higher stretch tends to open voids created in the spin bath. Wet stretch of from 3 to 6 ⁇ is preferred.
• the fibers produced by the above described process will generally be treated by "in-line relaxation” or batch annealing prior to final use.
• In-line relaxation is achieved by feeding the filaments into a hot water bath, usually 88° C. to boiling and withdrawing the filaments at a slower speed to compensate for shrinkage which takes place in the bath.
• the relaxed filaments are dried by conventional heated rolls or heated air and are suited for use as is or after being converted to staple without the need for a batch annealing process. This is a major advantage of the present invention since conventionally produced filaments require batch annealing.
• the filaments produced by the process of this invention can be subjected to conventional batch annealing processes in which case it is possible to obtain properties superior to those of conventional process filaments which have been batch annealed.
• This example which is provided for purposes of comparison, shows the preparation of an acrylic fiber product using a conventional commercial process and the properties of the resulting product.
• a 25% by weight solution of copolymer in a solvent consisting of 99.9% by weight DMAc and 0.1% by weight water is prepared.
• the copolymer contains 7.4 weight % vinyl acetate and 92.6% acrylonitrile.
• the copolymer contains 34 microequivalents per gram strong acid groups from the redox couple reaction.
• the solution is extruded at a rate of 109 liters/hour through a spinnerette having 40,000 0.076 millimeter diameter capillary openings into a coagulant bath containing 95 liters of a 52% by weight DMAc, 48% water mixture which is maintained at 38° C.
• the fibers formed are withdrawn from the coagulation bath by passage through a first roll set operating at a speed of 5.64 meters/minute to give a jet stretch ratio of 0.47 and are passed through water at 98° C. into a second roll set operating at a speed of 33.8 meters/minute to provide a wet stretch of 6 ⁇ .
• the fibers are annealed in a batch process by exposure to 35 PSIG (3.43 bar) steam for 20 minutes.
• a water emulsion of finish is circulated through the fiber bundle at 98° C. and the fibers dried by passage over a hot roll heated by 90 PSIG (7.22 bar) steam.
• the fibers produced are 5 denier per filament (5.5 decitex).
• the copolymer used in this example contains 34 microequivalents/gm strong acid groups and the W/S ratio of the coagulation bath is 4.47. Thus, Rho is calculated as being 0.26.
• the fiber produced is typical of conventional 5 dpf commercial fibers and has acceptable properties for use in flat woven upholstery and sweater fabrics.
• This example illustrates the production of acrylic fibers by the process of this invention and the properties of the products obtained.
• a 25% by weight solution of copolymer in a solvent consisting of 99.25% by weight DMAc and 0.75% by weight water is prepared.
• the copolymer contains 6.3 weight % vinyl acetate, 48 microequivalents per gm strong acid groups as a combination of polymer end groups and SPME comohomer and 93.4% acrylonitrile.
• the solution is extruded at a rate of 109 liters/hour through a spinnerette having 40,000 5 mil (0.076 millimeter) capillary openings into a coagulant bath containing 95 liters of a 71% by weight DMAc, 29% water mixture maintained at 30° C.
• the fibers formed are withdrawn from the coagulation bath by passage through a first roll set operating at a speed of 5.64 meters/minute to give a jet stretch ratio of 0.57 and are passed through 98° C. water into a second roll set operating at a speed 24.2 meters/minute to provide a wet stretch of 4.3 ⁇ .
• the fiber is provided in-line relaxation by passage from the second roll set through a 98° C. water bath into a third roll set of rolls operating at a speed of 65 ft/min (19.8 meters/minute). No batch process annealing is provided. Finish is applied as in Example 1 and the fibers dried by passage of a roll heated with 90 PSIG (7.22 bar) steam. The resulting fiber product is 5 denier per filament (5.5 decitex).
• the polymer used has a strong acid group concentration of 48 microequivalents per gram and the W/S ratio of the coagulation bath is 1.97. thus, Rho is calculated as being 1.09.
• a fabric made from staple yarn made from fibers produced via this example withstands over twice as many cycles as fabric made from staple spun from fibers produced according to Example 1.
• This example compares a product produced by the process of this invention and subjected to batch process annealing with a conventional bath process annealed product.
• a 25% by weight solution of a copolymer in a solvent consisting of 99.25% DMAc and 0.75% water is prepared.
• the copolymer contains 6.3 weight % vinyl acetate and 93.7% acrylonitrile with 48 microequivalents/gm strong acid end groups from the redox couple polymerization.
• the solution is extruded at a rate of 93 liters/hour through a spinnerette having 60,000 2.5 mil (0. 063 millimeter) capillary openings into a coagulant bath containing 95 liters of a 69% DMAc, 31% water mixture which is maintained at 30° C.
• the fibers are withdrawn from the coagulation bath with a jet stretch ratio of 0.48 and given a 4.77 wet stretch. Finish is applied as in previous examples and the fibers dried.
• the fibers are batch annealed by exposure to 40 PSIG (3.77 bar) steam for 20 minutes.
• the resulting fibers are 5 denier per filament (5.5 decitex).
• the polymer used contains 48 microequivalents/gm strong acid groups and the W/S ratio of the coagulation bath is 2.17. Rho is calculated as being 0.998.
• the copolymer dope is a 25% solution of copolymer in a solvent consisting of 99.9% DMAc and 0.1% water.
• the copolymer contains 7.4 weight % vinyl acetate, 34 microequivalents of strong acid groups from the redox couple acrylonitrile polymerization system and 92.6% acrylonitrile.
• the coagulation bath is a mixture of 52% DMAc and 48% water maintained at 35° C.
• the fiber is withdrawn at a jet stretch of 0.59 and wet stretched 5.66 ⁇ .
• the resulting product is 5 denier per filament (5.5 decitex) and has a calculated Rho of 0.26.

Landscapes

• Health & Medical Sciences (AREA)
• Toxicology (AREA)
• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Artificial Filaments (AREA)

Priority Applications (9)

Applications Claiming Priority (1)

Publications (1)

Family

ID=23133772

Family Applications (1)

Country Status (9)

Cited By (3)

Families Citing this family (2)

Citations (15)

Family Cites Families (8)

• 1994
  • 1994-08-23 US US08/294,516 patent/US5496510A/en not_active Expired - Lifetime
• 1995
  • 1995-08-03 KR KR1019970701109A patent/KR970705659A/ko not_active Withdrawn
  • 1995-08-03 MX MX9701365A patent/MX9701365A/es unknown
  • 1995-08-03 EP EP95927567A patent/EP0777769A1/en not_active Withdrawn
  • 1995-08-03 WO PCT/US1995/009873 patent/WO1996006209A1/en not_active Application Discontinuation
  • 1995-08-03 BR BR9508755A patent/BR9508755A/pt not_active Application Discontinuation
  • 1995-08-03 JP JP8508097A patent/JPH10504616A/ja active Pending
  • 1995-08-16 PE PE1995276403A patent/PE43896A1/es not_active Application Discontinuation
  • 1995-08-24 TW TW084108828A patent/TW277077B/zh active

Patent Citations (16)

Also Published As

Similar Documents

Legal Events